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rs864622600

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs864622600(-;A)
Make rs864622600(A;A)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position5987014
GenePMS2
is asnp
is mentioned by
dbSNPrs864622600
dbSNP (old)rs864622600
ClinGenrs864622600
ebirs864622600
HLIrs864622600
Exacrs864622600
Gnomadrs864622600
Varsomers864622600
Maprs864622600
PheGenIrs864622600
Biobankrs864622600
1000 genomesrs864622600
hgdprs864622600
ensemblrs864622600
gopubmedrs864622600
geneviewrs864622600
scholarrs864622600
googlers864622600
pharmgkbrs864622600
gwascentralrs864622600
openSNPrs864622600
23andMers864622600
23andMe allrs864622600
SNP Nexus

SNPshotrs864622600
SNPdbers864622600
MSV3drs864622600
GWAS Ctlgrs864622600
Max Magnitude0
ClinVar
Risk rs864622600(A;A)
Alt rs864622600(A;A)
Reference Rs864622600(-;-)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene PMS2
CLNDBN Lynch syndrome
Reversed 1
HGVS NC_000007.13:g.6026646dupT
CLNSRC
CLNACC RCV000203802.2,